dc.contributor |
Ziegler, Thomas |
de_CH |
dc.contributor.author |
Ziegler, Thomas |
de_DE |
dc.contributor.author |
Hürttlen, Jürgen |
de_DE |
dc.date.accessioned |
2006-05-11 |
de_DE |
dc.date.accessioned |
2014-03-18T10:15:41Z |
|
dc.date.available |
2006-05-11 |
de_DE |
dc.date.available |
2014-03-18T10:15:41Z |
|
dc.date.issued |
2006 |
de_DE |
dc.identifier.other |
394492404 |
de_DE |
dc.identifier.uri |
http://nbn-resolving.de/urn:nbn:de:bsz:21-opus-22912 |
de_DE |
dc.identifier.uri |
http://hdl.handle.net/10900/48917 |
|
dc.description.abstract |
An asymmetric o-methylbenzoyl tether for intramolecular glycosylations is prepared from o-methoxycarbonyl-benzylidene glucosamine by benzylation, saponification, condensation with phenyl 3,4,6-benzyl-1-thio-glucoside, and regioselective ring opening of the benzylidene moiety. Thus obtained prearranged glycoside affords the corresponding beta(1,4)-linked disaccharide as the major product. |
en |
dc.language.iso |
en |
de_DE |
dc.publisher |
Universität Tübingen |
de_DE |
dc.rights |
ubt-podno |
de_DE |
dc.rights.uri |
http://tobias-lib.uni-tuebingen.de/doku/lic_ohne_pod.php?la=de |
de_DE |
dc.rights.uri |
http://tobias-lib.uni-tuebingen.de/doku/lic_ohne_pod.php?la=en |
en |
dc.subject.classification |
Glykosylierung , Intramolekulare Reaktion , Glykoside |
de_DE |
dc.subject.ddc |
540 |
de_DE |
dc.subject.other |
Glycosylierung , Intramolekulare Reaktion , vorverbrückte Glycoside |
de_DE |
dc.subject.other |
glycosylation , intramolecular , prearranged glycosides |
en |
dc.title |
Prearranged glycosides part 16. Non-symmetrically tethered glycosides via o-Hydroxycarbonyl-benzylidene-glycosides |
en |
dc.type |
WorkingPaper |
de_DE |
utue.publikation.fachbereich |
Sonstige - Chemie und Pharmazie |
de_DE |
utue.publikation.fakultaet |
7 Mathematisch-Naturwissenschaftliche Fakultät |
de_DE |
dcterms.DCMIType |
Text |
de_DE |
utue.publikation.typ |
workingPaper |
de_DE |
utue.opus.id |
2291 |
de_DE |
utue.publikation.source |
keine |
de_DE |